cerca per
pagina 1
- Location: Nestlé Institute of Health Sciences - EPFL site, SwitzerlandEntity: Nestlé Research, Société des Produits Nestlé S.A.Act. Rate: Full-Time Act. Rate 100%Contract type: TemporaryDesired start date: January 5th, 2026End of assignment: December 31st, 2026Nestlé Research is based in Lausanne, Switzerland, employs approximately 1000 people and is comprised of five Nestlé Institutes: Food Sciences, Health Sciences, Food Safety & Analytical Sciences,Location: Nestlé Institute of Health Sciences - EPFL site, SwitzerlandEntity: Nestlé Research, Société des Produits Nestlé S.A.Act. Rate: Full-Time Act. Rate 100%Contract type: TemporaryDesired start date: January 5th, 2026End of assignment: December 31st, 2026Nestlé Research is based in Lausanne, Switzerland, employs approximately 1000 people and is comprised of five Nestlé Institutes: Food Sciences, Health Sciences, Food Safety & Analytical Sciences,
- For one of our clients, a global manufacturing company specialized in the life sciences sector, we are looking for a Manufacturing Scientist based in the canton of Fribourg. Your Impact:Implement and optimize robust, compliant, and high-performing manufacturing processes aligned with quality strategyCapitalize on and share your expertise throughout the entire product lifecycleDraft, review, and approve key technical documents (batch records, procedures,For one of our clients, a global manufacturing company specialized in the life sciences sector, we are looking for a Manufacturing Scientist based in the canton of Fribourg. Your Impact:Implement and optimize robust, compliant, and high-performing manufacturing processes aligned with quality strategyCapitalize on and share your expertise throughout the entire product lifecycleDraft, review, and approve key technical documents (batch records, procedures,
- For one of our clients, a world leader in in-vitro diagnostics, we are currently looking for a Product Safety Specialist - Electronic Diagnostics Instruments.General Information: Start date: asapLatest possible start date: 01.02.2026Duration: 1 year with the possibility of extensionWorkplace: Rotkreuz Workload: 80-100%Remote/Home Office: possible, at least 3 days on site work per week is expectedWorking hours: StandardDepartment: Compliance Operations,For one of our clients, a world leader in in-vitro diagnostics, we are currently looking for a Product Safety Specialist - Electronic Diagnostics Instruments.General Information: Start date: asapLatest possible start date: 01.02.2026Duration: 1 year with the possibility of extensionWorkplace: Rotkreuz Workload: 80-100%Remote/Home Office: possible, at least 3 days on site work per week is expectedWorking hours: StandardDepartment: Compliance Operations,
- About the roleWe’re looking for a CQV Engineer to drive the validation of equipment, systems, and facilities in a regulated pharmaceutical environment. You will coordinate installations, author and execute IQ/OQ/PQ protocols, and document results in compliance with cGMP/GxP requirements—ensuring our operations are safe, compliant, and inspection-ready.What you’ll doPlan and coordinate CQV activities for facilities & utilities (e.g., HVAC, cleanrooms, WFI,About the roleWe’re looking for a CQV Engineer to drive the validation of equipment, systems, and facilities in a regulated pharmaceutical environment. You will coordinate installations, author and execute IQ/OQ/PQ protocols, and document results in compliance with cGMP/GxP requirements—ensuring our operations are safe, compliant, and inspection-ready.What you’ll doPlan and coordinate CQV activities for facilities & utilities (e.g., HVAC, cleanrooms, WFI,
- For our client, a leading biotechnology company based in canton Zug, we are seeking a Regulatory Affairs Manager. General Information: Start date: ASAPEnd date: 30/06/2026Contract: temporary contract via RandstadWorkplace: Baar, ZugWorkload: 100%Working hours: StandardTask & Responsibilities: Responsible for managing the development and implementation of regulatory strategy for specific projects and programs. Contribute to identification and assessment ofFor our client, a leading biotechnology company based in canton Zug, we are seeking a Regulatory Affairs Manager. General Information: Start date: ASAPEnd date: 30/06/2026Contract: temporary contract via RandstadWorkplace: Baar, ZugWorkload: 100%Working hours: StandardTask & Responsibilities: Responsible for managing the development and implementation of regulatory strategy for specific projects and programs. Contribute to identification and assessment of
- Location: Bulle, SwitzerlandActivity rate : 100%Type of contract: Temporary contractStart date: 05.01.2026End date: 30.06.2026 (potential extensions)We are looking for an experienced Electronic Data Integrity QA Specialist to join the Quality Assurance team of UCB.In this role, you will act as a QA subject matter expert in data integrity, computerized system validation (CSV), and automation within a biotech manufacturing environment. You will review andLocation: Bulle, SwitzerlandActivity rate : 100%Type of contract: Temporary contractStart date: 05.01.2026End date: 30.06.2026 (potential extensions)We are looking for an experienced Electronic Data Integrity QA Specialist to join the Quality Assurance team of UCB.In this role, you will act as a QA subject matter expert in data integrity, computerized system validation (CSV), and automation within a biotech manufacturing environment. You will review and
